JP2012532883A5 - - Google Patents

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Publication number
JP2012532883A5
JP2012532883A5 JP2012519731A JP2012519731A JP2012532883A5 JP 2012532883 A5 JP2012532883 A5 JP 2012532883A5 JP 2012519731 A JP2012519731 A JP 2012519731A JP 2012519731 A JP2012519731 A JP 2012519731A JP 2012532883 A5 JP2012532883 A5 JP 2012532883A5
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Japan
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compound according
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JP2012519731A
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English (en)
Japanese (ja)
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JP5925121B2 (ja
JP2012532883A (ja
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Priority claimed from PCT/US2010/041379 external-priority patent/WO2011005969A2/en
Publication of JP2012532883A publication Critical patent/JP2012532883A/ja
Publication of JP2012532883A5 publication Critical patent/JP2012532883A5/ja
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Publication of JP5925121B2 publication Critical patent/JP5925121B2/ja
Expired - Fee Related legal-status Critical Current
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JP2012519731A 2009-07-10 2010-07-08 副腎皮質ステロイド合成を阻害しないエトミデート類似体 Expired - Fee Related JP5925121B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22475109P 2009-07-10 2009-07-10
US61/224,751 2009-07-10
PCT/US2010/041379 WO2011005969A2 (en) 2009-07-10 2010-07-08 Etomidate analogues that do not inhibit adrenocortical steroid synthesis

Publications (3)

Publication Number Publication Date
JP2012532883A JP2012532883A (ja) 2012-12-20
JP2012532883A5 true JP2012532883A5 (pl) 2013-08-22
JP5925121B2 JP5925121B2 (ja) 2016-05-25

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ID=43429834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012519731A Expired - Fee Related JP5925121B2 (ja) 2009-07-10 2010-07-08 副腎皮質ステロイド合成を阻害しないエトミデート類似体

Country Status (10)

Country Link
US (2) US8765973B2 (pl)
EP (1) EP2451779B1 (pl)
JP (1) JP5925121B2 (pl)
CN (1) CN102548964B (pl)
AU (1) AU2010271345B2 (pl)
BR (1) BR112012000606A2 (pl)
CA (1) CA2767112C (pl)
HK (1) HK1172026A1 (pl)
RU (1) RU2559888C2 (pl)
WO (1) WO2011005969A2 (pl)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014017230A2 (pt) * 2012-01-13 2020-11-24 The General Hospital Corporation compostos anestésicos e métodos de uso relacionados
US9637469B2 (en) * 2012-11-14 2017-05-02 Teijin Pharma Limited Pyridine derivative
US20180022698A1 (en) 2014-10-16 2018-01-25 The Board Of Trustees Of The Leland Stanford Junior University Novel methods, compounds, and compositions for anesthesia
IL258525B2 (en) 2015-10-07 2023-03-01 Apellis Pharmaceuticals Inc Dosing regimens
JP6983416B2 (ja) * 2015-10-10 2021-12-17 ジアンス・エンファルオカン・ファーマスーティカル・リサーチ・アンド・デベロップメント・カンパニー・リミテッドJiangsu Nhwaluokang Pharmceutical Research And Development Co., Ltd. エトミデート誘導体ならびにその中間体、調製方法および使用
CN107445898A (zh) * 2016-05-30 2017-12-08 四川海思科制药有限公司 N‑取代咪唑羧酸酯类化合物及其制备方法和在医药上的用途
CN107522662A (zh) * 2016-06-16 2017-12-29 四川海思科制药有限公司 N‑取代咪唑羧酸酯类化合物及其制备方法和在医药上的用途
CN107641105A (zh) * 2016-07-22 2018-01-30 四川海思科制药有限公司 N‑取代咪唑羧酸酯类化合物及其制备方法和在医药上的用途
CN107652239B (zh) * 2017-02-24 2020-08-04 四川大学华西医院 N-取代咪唑羧酸酯类化合物、制备方法及用途
EP3606465A4 (en) 2017-04-07 2021-03-24 Apellis Pharmaceuticals, Inc. DOSING PLANS, ASSOCIATED COMPOSITIONS AND PROCEDURES
CN109776509B (zh) 2018-01-30 2023-07-07 成都麻沸散医药科技有限公司 一种n-取代咪唑甲酸酯类衍生物及其用途
CN110003188B (zh) * 2019-03-27 2022-08-26 成都麻沸散医药科技有限公司 取代吡咯甲酸酯类衍生物及其用途
CN110669017B (zh) * 2019-10-11 2023-08-04 成都麻沸散医药科技有限公司 多取代***甲酸酯类衍生物及其用途
CN112174890B (zh) * 2020-10-09 2022-05-27 成都麻沸散医药科技有限公司 酮取代杂环化合物及其麻醉作用

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US3354173A (en) 1964-04-16 1967-11-21 Janssen Pharmaceutica Nv Imidazole carboxylates
US4038286A (en) 1975-03-10 1977-07-26 Janssen Pharmaceutica N.V. Racemates and optical isomers of 1-(1-phenylethyl)-1h-imidazole-5-carboylic acid derivatives
GR64915B (en) 1978-09-14 1980-06-09 Janssen Pharmaceutica Nv Improved etomidate-containing compositions
US4878940A (en) 1987-04-02 1989-11-07 Janssen Pharmaceutica N.V. Herbicidal 1,5-substituted 1H-imidazoles
CA2008616C (en) * 1989-01-31 2000-07-18 Roger A. Parker Aryl- or heteroaryl-1-alkyl-pyrrole-2-carboxylic acid compounds useful in treating interleukin-1 mediated conditions
US5041554A (en) * 1989-01-31 1991-08-20 Merrell Dow Pharmaceuticals Inc. Novel aryl-or heteroaryl-1-alkyl-pyrrole-2-carboxylic acid compounds useful in treating interleukin-1 mediated conditions
US5019583A (en) 1989-02-15 1991-05-28 Glaxo Inc. N-phenyl-N-(4-piperidinyl)amides useful as analgesics
US5242939A (en) * 1990-09-28 1993-09-07 Warner-Lambert Company Anilide derivatives with angiotensin ii antagonist properties
JP3374922B2 (ja) 1991-05-09 2003-02-10 日産化学工業株式会社 複素環式第3級アミンの製造方法
JPH06345728A (ja) 1993-06-11 1994-12-20 Nissan Chem Ind Ltd N−置換アゾール誘導体の製造方法
US5466700A (en) 1993-08-30 1995-11-14 Glaxo Wellcome Inc. Anesthetic use of N-phenyl-N-(4-piperidinyl)amides
US5756528A (en) 1995-06-06 1998-05-26 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
RU2160265C1 (ru) * 2000-03-17 2000-12-10 Научно-исследовательский институт физической и органической химии Ростовского государственного университета Дигидрохлорид 1-(3-пирролидинопропил)-2-фенилимидазо [1,2-а]-бензимидазола, обладающий местноанестезирующим действием
AU2002254309B2 (en) 2001-03-20 2006-02-02 Cydex, Inc. Formulations containing propofol and a sulfoalkyl ether cyclodextrin
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EP1778652A2 (en) 2004-08-20 2007-05-02 EntreMed, Inc. Compositions and methods comprising proteinase activated receptor antagonists
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